Methylamine → HCID 20248698, compound
Reaction equation
[C:1]1([C:7](=[O:20])[CH:8]([CH3:19])[CH2:9][C:10]2[CH:15]=[CH:14][C:13]([N:16]=[C:17]=[O:18])=[CH:12][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:21][NH2:22]>C1(C)C=CC=CC=1>[C:1]1([C:7](=[O:20])[CH:8]([CH3:19])[CH2:9][C:10]2[CH:11]=[CH:12][C:13]([NH:16][C:17]([NH:22][CH3:21])=[O:18])=[CH:14][CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 40 °C
Procedure
A solution of 13.25 g of 4-(3-phenyl-2-methyl-n-propan-3-onyl)-phenyl isocyanate in 20 ml of toluene was added dropwise to a solution of 3 g of methylamine in 100 ml of toluene, at from 20° to 25° C. The mixture was stirred for 6 hours at 40° C., after which the toluene was stripped off under reduced pressure. 13.3 g (90% of theory) of a slightly yellow oil were obtained.
Workup
- custom13.3 g (90% of theory) of a slightly yellow oil were obtained
Sources & evidence
- ORD record
- ord-c0fe12d36bfb4abf864ef1de1c402ab7
- Source dataset
- uspto-grants-1986_01
- Patent number
- US04566900
Reaction notes
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